MEASUREMENT OF BACTERIAL RANDOM MOTILITY AND CHEMOTAXIS COEFFICIENTS .1. STOPPED-FLOW DIFFUSION CHAMBER ASSAY

被引:97
作者
FORD, RM [1 ]
PHILLIPS, BR [1 ]
QUINN, JA [1 ]
LAUFFENBURGER, DA [1 ]
机构
[1] UNIV PENN,DEPT CHEM ENGN,PHILADELPHIA,PA 19104
关键词
BACTERIAL CHEMOTAXIS; ESCHERICHIA-COLI; MOTILITY; RANDOM; DIFFUSION CHAMBER ASSAY; MATHEMATICAL MODEL;
D O I
10.1002/bit.260370707
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Bacterial chemotaxis, the directed movement of a cell population in response to a chemical gradient, plays a critical role in the distribution and dynamic interaction of bacterial populations in nonmixed systems. Therefore, in order to make reliable predictions about the migratory behavior of bacteria within the environment, a quantitative characterization of the chemotactic response in terms of intrinsic cell properties is needed. The design of the stopped-flow diffusion chamber (SFDC) provides a well-characterized chemical gradient and reliable method for measuring bacterial migration behavior. During flow through the chamber, a step change in chemical concentration is imposed on a uniform suspension of bacteria. Once flow is stopped, diffusion causes a transient chemical gradient to develop, and bacteria respond by forming a band of high cell density which travels toward higher concentrations of the attractant. Changes in bacterial spatial distributions observed through light scattering are recorded on photomicrographs during a 10-min period. Computer-aided image analysis converts absorbance of the photographic negatives to a digital representation of bacterial density profiles. A mathematical model (part II) is used to quantitatively characterize these observations in terms of intrinsic cell parameters: a chemotactic sensitivity coefficient, chi-0, from the aggregate cell density accumulated in the band and a random motility coefficient, mu, from population dispersion in the absence of a chemical gradient. Using the SFDC assay and an individual-cell-based mathematical model, we successfully determined values for both of these population parameters for Escherichia coli K12 responding to fucose. The values obtained were mu = 1.1 +/- 0.4 x 10(-5) cm2/s and chi-0 = 8 +/- 3 x 10(-5) cm2/s. We have demonstrated a method capable of determining these parameter values from the now validated mathematical model which will be useful for predicting bacterial migration in application systems.
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收藏
页码:647 / 660
页数:14
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